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Showing results (101-110 of 170) with videos related to

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Molecular and Cellular Biochemistry|April 18, 2021
Cartiotonic steroids affect monolayer permeability in lymphatic endothelial cellsDarijana Horvat, Syeda H Afroze, Walter E Cromer, et al.
Journal of Medical Genetics|August 7, 2007
Deletions or duplications in KCNQ2 can cause benign familial neonatal seizuresS E Heron, K Cox, B E Grinton, et al.
Epilepsia Open|March 29, 2018
Classification of the epilepsies: New concepts for discussion and debate-Special report of the ILAE Classification Task Force of the Commission for Classification and TerminologyIngrid E Scheffer, Jacqueline French, Edouard Hirsch, et al.
Epilepsia Open|July 8, 2022
An examination of the efficacy and safety of fenfluramine in adults, children, and adolescents with Dravet syndrome in a real-world practice setting: A report from the Fenfluramine European Early Access ProgramRenzo Guerrini, Nicola Specchio, Ángel Aledo-Serrano, et al.
Epilepsy & Behavior Reports|November 16, 2020
Infantile spasms: Etiology, lead time and treatment response in a resource limited settingPriyanka Surana, Joseph D Symonds, Prabhar Srivastava, et al.
JAMA Network Open|April 16, 2024
Treatments and Outcomes Among Patients with Sydenham Chorea: A Meta-AnalysisMichael Eyre, Terrence Thomas, Emanuela Ferrarin, et al.
Clinical & Translational Oncology : Official Publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico|November 11, 2015
Clinical significance of TP53 (R72P) and MDM2 (T309G) polymorphisms in breast cancer patientsP Yadav, M Masroor, K Tanwer, et al.
The New England Journal of Medicine|May 17, 2018
Effect of Cannabidiol on Drop Seizures in the Lennox-Gastaut SyndromeOrrin Devinsky, Anup D Patel, J Helen Cross, et al.
The Lancet. Neurology|May 23, 2006
De-novo mutations of the sodium channel gene SCN1A in alleged vaccine encephalopathy: a retrospective studySamuel F Berkovic, Louise Harkin, Jacinta M McMahon, et al.
Human Mutation|November 30, 2019
SCN1A variants from bench to bedside-improved clinical prediction from functional characterizationAndreas Brunklaus, Stephanie Schorge, Alexander D Smith, et al.
Pageof 17

Showing results (101-110 of 170) with videos related to

Sort By:
Pageof 17
Molecular and Cellular Biochemistry|April 18, 2021
Cartiotonic steroids affect monolayer permeability in lymphatic endothelial cellsDarijana Horvat, Syeda H Afroze, Walter E Cromer, et al.
Journal of Medical Genetics|August 7, 2007
Deletions or duplications in KCNQ2 can cause benign familial neonatal seizuresS E Heron, K Cox, B E Grinton, et al.
Epilepsia Open|March 29, 2018
Classification of the epilepsies: New concepts for discussion and debate-Special report of the ILAE Classification Task Force of the Commission for Classification and TerminologyIngrid E Scheffer, Jacqueline French, Edouard Hirsch, et al.
Epilepsia Open|July 8, 2022
An examination of the efficacy and safety of fenfluramine in adults, children, and adolescents with Dravet syndrome in a real-world practice setting: A report from the Fenfluramine European Early Access ProgramRenzo Guerrini, Nicola Specchio, Ángel Aledo-Serrano, et al.
Epilepsy & Behavior Reports|November 16, 2020
Infantile spasms: Etiology, lead time and treatment response in a resource limited settingPriyanka Surana, Joseph D Symonds, Prabhar Srivastava, et al.
JAMA Network Open|April 16, 2024
Treatments and Outcomes Among Patients with Sydenham Chorea: A Meta-AnalysisMichael Eyre, Terrence Thomas, Emanuela Ferrarin, et al.
Clinical & Translational Oncology : Official Publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico|November 11, 2015
Clinical significance of TP53 (R72P) and MDM2 (T309G) polymorphisms in breast cancer patientsP Yadav, M Masroor, K Tanwer, et al.
The New England Journal of Medicine|May 17, 2018
Effect of Cannabidiol on Drop Seizures in the Lennox-Gastaut SyndromeOrrin Devinsky, Anup D Patel, J Helen Cross, et al.
The Lancet. Neurology|May 23, 2006
De-novo mutations of the sodium channel gene SCN1A in alleged vaccine encephalopathy: a retrospective studySamuel F Berkovic, Louise Harkin, Jacinta M McMahon, et al.
Human Mutation|November 30, 2019
SCN1A variants from bench to bedside-improved clinical prediction from functional characterizationAndreas Brunklaus, Stephanie Schorge, Alexander D Smith, et al.
Pageof 17